Clinical Performance of B-Lite® Light Weight Breast Implant

  • End date
    Dec 26, 2025
  • participants needed
  • sponsor
    G&G Biotechnology Ltd.
Updated on 26 January 2022
Accepts healthy volunteers


This is a post-marketing study for B-Lite implants that carry the EC certificate for marketing in Europe and AMAR certificate for marketing in Israel. To date, thousands of implants have already been implanted in women. The study is open for primary augmentation patients only. All surgeries will be performed as per standard practice at the given study site. No parallel surgical procedures will be performed at the same session.

Condition Breast Implants
Treatment B-Lite- Light Weight Breast Implants
Clinical Study IdentifierNCT02777476
SponsorG&G Biotechnology Ltd.
Last Modified on26 January 2022


Yes No Not Sure

Inclusion Criteria

Genetic women between the ages of 18 and 60 seeking primary breast augmentation
Patient is eligible to undergo MRI (i.e., no implanted metal or metal devices, no history of severe claustrophobia)
Patient provides signed informed consent
Patient agrees to comply with the study protocol and complete all required follow up visits, including to undergo MRI
Patient agrees to return the device to the Sponsor should the implant have to be explanted
The patient has realistic expectations of surgical results after discussion with investigator and is an acceptable candidate for breast augmentation

Exclusion Criteria

Patients with active infection anywhere in their body
Patient is pregnant or nursing at the time of recruitment, or has been in the 6 months preceding recruitment date, or not willing to use reliable means of contraception during the first year after surgery
Patient was implanted with any silicone implant other than breast implants (e.g., silicone artificial joints or facial implants)
Patient breast tissue is clinically incompatible for the procedure (e.g., tissue damage resulting from radiation, insufficient tissue coverage or compromised vascularity)
Patient has a condition, or is under treatment for any condition, which, in the opinion of the investigator and/or consulting physician(s), may constitute an unwarranted surgical risk (e.g., unstable cardiac or pulmonary problems, possible allergies and/or extraordinary immune response to implant)
The patient has a history of mental instability and/or history of pharmaceutical psychiatric treatment
Patient unable to understand the scope of the study and/or surgery
The patient has any disease, including uncontrolled diabetes (e.g., HbA1c > 8%), that is clinically known to impact wound healing ability
Patient has existing costal injuries
Patient has abscesses, malignant tumors (cancer or recurrent metastases), clinically relevant cysts or advanced fibrotic disease or patient with BIRAD 3
Are not willing to undergo further surgery for revision, if medically required
The patient has a confirmed rheumatic disease or syndrome (e.g., SLE, Sjogren's syndrome, scleroderma, polymyositis or any connective tissue disorder, rheumatoid arthritis, crystalline arthritis, infectious arthritis, spondyloarthropathies, any other inflammatory arthritis, fibromyalgia or chronic fatigue syndrome)
The patient has a severe breast and upper trunk deformity
The patient participated in an investigational trial within 90 days of enrollment
The patient has undergone an invasive medical procedure within 90 days of enrollment
Aesthetic addiction, drug abuse, alcohol abuse
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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